A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528283



Internal ID15455576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:100506007..100506160hg38UCSC Ensembl
Innerchr6:100953883..100954036hg19UCSC Ensembl
Innerchr6:101060604..101060757hg18UCSC Ensembl
Innerchr6:101060604..101060757hg17UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg38154
hg19154
hg18154
hg17154
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704853
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528283
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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